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Double Cushion BK SiloSheath, Size 7

FDA UDI

Class I (US FDA UDI)

by SILIPOS Holding LLC

Identity

Trade Name
Double Cushion BK SiloSheath, Size 7 FDA UDI
Generic Name
External limb prosthesis socket liner FDA UDI
Model / Reference
13475 FDA UDI

Identifiers

Primary DI / UDI-DI
00614464134753 FDA UDI
FDA Product Code
IPM FDA UDI
GMDN Term
External limb prosthesis socket liner FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3025 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: External limb prosthesis socket liner

Double Cushion BK SiloSheath, Size 7 by SILIPOS Holding LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External limb prosthesis socket liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SILIPOS Holding LLC

Sources (1)

  • FDA UDI c0221222-3261-48f2-8d26-73f46188eeba 32 fields · synced Jun 1, 2026